Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
12991 to 13000 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

12991
Syntaxin 12
STX13, STX14
Diabetes mellitus type 2

12992
Syntaxin 16
SYN-16, SYN16
Pseudohypoparathyroidism

12993
Syntaxin 17
-
Insomnia, Melanoma

12994
Syntaxin 18
Ufe1
Scoliosis

12995
Syntaxin 1A
HPC-1, P35-1, STX1, SYN1A
Autism, Neurodevelopmental disorder, Creutzfeldt-jakob disease, Cystic fibrosis, Hirschsprung disease, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Schizophrenia, Williams syndrome

12996
Syntaxin 1B
GEFSP9, STX1B1, STX1B2
Epilepsy, Generalized epilepsy, Developmental and epileptic encephalopathy, Febrile convulsion, Generalized epilepsy with febrile seizures plus, Neurodevelopmental disorder, Neurotic disorder, Parkinson disease, Psoriasis, Psoriasis vulgaris, Seizures, Diabetes mellitus type 2

12997
Syntaxin 2
EPIM, EPM, STX2A, STX2B, STX2C
Central nervous system cancer, Coronary artery disease, Glioblastoma, Glioma, Male infertility, Renal pelvis neoplasms, Spermatogenic failure, Venous thromboembolism

12998
Syntaxin 3
DIAR12, MVID2, RDMVID, STX3A
Color vision deficiency, Microvillus inclusion disease

12999
Syntaxin 4
DFNB123, STX4A, p35-2
Isolated sensorineural deafness, Deafness, Hearing loss, Psoriasis, Nonsyndromic hearing loss, Diabetes mellitus type 2

13000
Syntaxin 5
CDG2AA, SED5, STX5A
Congenital disorder of glycosylation